Ekta Rai - Publications

ESR1 as a candidate gene for adolescent idiopathic scoliosis pathogenesis in North-West Indian population.

Journal: European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society

Published: April 07, 2026

SBSPON gene association with type 2 diabetes mellitus and its impact on leukocyte telomere length.

Journal: Frontiers in endocrinology

Published: February 06, 2026

ARL15 Gene Variant rs255758 Provides Susceptibility to Rheumatoid Arthritis in Northwest Indian Population.

Journal: International journal of applied & basic medical research

Published: April 06, 2024

Bergenin inhibits growth of human cervical cancer cells by decreasing Galectin-3 and MMP-9 expression.

Journal: Scientific reports

Published: December 04, 2023

SOX9 gene shows association with adolescent idiopathic scoliosis predisposition in Northwest Indians.

Journal: European journal of medical research

Published: October 14, 2023

Cost-effective Whole Exome Sequencing discovers pathogenic variant causing Neurofibromatosis type 1 in a family from Jammu and Kashmir, India.

Journal: Scientific reports

Published: May 18, 2022

The first study of epidemiology of adolescent idiopathic scoliosis shows lower prevalence in females of Jammu and Kashmir, India.

Journal: American journal of translational research

Published: July 25, 2021

LRFN2 gene variant rs2494938 provides susceptibility to esophageal cancer in the population of Jammu and Kashmir.

Journal: Journal of cancer research and therapeutics

Published: September 04, 2020

Dual labeled fluorescence probe based qPCR assay to measure the telomere length.

Journal: Gene

Published: August 27, 2020

Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir - India.

Journal: Frontiers in genetics

Published: August 03, 2019

Telomere Maintenance Genes are associated with Type 2 Diabetes Susceptibility in Northwest Indian Population Group.

Journal: Scientific reports

Published: May 21, 2019

A case report on a novel MT-ATP6 gene variation in atypical mitochondrial Leigh syndrome associated with bilateral basal ganglia calcifications.

Journal: Mitochondrion

Published: January 08, 2018